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Correction: In vitro vascularized liver tumor model based on a microfluidic inverse opal scaffold for immune cell recruitment investigation
Pingwei Xua,
Junjie Chi*a,
Xiaochen Wangabc,
Meng Zhud,
Kai Chene,
Qihui Fan*c,
Fangfu Ye*abc and
Changmin Shao*ab
aJoint Centre of Translational Medicine, The First Affiliated Hospital of Wenzhou Medical University, Wenzhou 325035, China. E-mail: cjj_2337@163.com; changmin_shao@163.com
bWenzhou Institute, University of Chinese Academy of Sciences, Wenzhou 325001, China
cBeijing National Laboratory for Condensed Matter Physics, Institute of Physics, Chinese Academy of Sciences, Beijing 100190, China
dThe First Clinical Medical College, Wenzhou Medical University, Wenzhou 325035, China
eDepartment of Hepatobiliary and Pancreatic Surgery, The First Affiliated Hospital of Wenzhou Medical University, Wenzhou 325035, China
First published on 26th February 2025
Abstract
Correction for ‘In vitro vascularized liver tumor model based on a microfluidic inverse opal scaffold for immune cell recruitment investigation’ by Pingwei Xu et al., Lab Chip, 2024, 24, 3470–3479, https://doi.org/10.1039/D4LC00341A
In the above article, the authors regret that Fig. 5a was incorrectly labelled. The correct version of Fig. 5 is shown here.
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| Fig. 5 The 3D co-culture system promotes immune suppression on neutrophils to support tumor progression. (a) The recruitment of immune cells in vivo was analyzed by flow cytometry. (b) The recruitment of neutrophils in vitro was analyzed by the transwell assay. (c and d) The expression of CXCL1 and CXCL2 in tumor cells was analyzed by real-time PCR and ELISA. (e and f) The population (e) and count (f) of tumor cells were analyzed by flow cytometry. (g) Analysis of the long-term survival rate of mice. *P < 0.05, **P < 0.01, ****P < 0.0001. | ||
The Royal Society of Chemistry apologises for these errors and any consequent inconvenience to authors and readers.
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